Cholecystitis

Symptom Information:

Symptom ID: HPO:0001082
Synonyms:
Cholecystitis (disorder) [Orphanet:29060]
Cholecystitis [Orphanet:29060]
Cholecystitis [OMIM:Cholecystitis]
Biliary/gallbladder stones/lithiasis/cholecystitis [Orphanet:29060]
Cholecystitis [MedDRA:10008612]
Acalculous cholecystitis [MedDRA:10008612]
Calculus of gallbladder with other cholecystitis [MedDRA:10008612]
Calculus of gallbladder with other cholecystitis, with obstruction [MedDRA:10008612]
Calculus of gallbladder with other cholecystitis, without mention of obstruction [MedDRA:10008612]
Cholecystitis (alone) [MedDRA:10008612]
Cholecystitis NOS [MedDRA:10008612]
Cholecystitis, other [MedDRA:10008612]
Gallbladder inflammation [MedDRA:10008612]
Inflammation gallbladder [MedDRA:10008612]
Other cholecystitis [MedDRA:10008612]
Calculous cholecystitis [MedDRA:10008612]
Quality:
Cross references:
Orphanet:29060 "Biliary/gallbladder stones/lithiasis/cholecystitis" [Orphanet:29060]
OMIM: "Cholecystitis" [OMIM:Cholecystitis]
UMLS:C1963083 "Cholecystitis" [HPO:0001082]
UMLS:C0008325 "Cholecystitis" [Orphanet:29060]
Is a (Direct Parents):
Orphanet Cholelithiasis
HPO         Abnormal gallbladder physiology
MedDRA Cholecystitis and cholelithiasis
Orphanet Decreased liver function
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the liver(HPO:0001392)
                Abnormality of the biliary system(HPO:0004297)
                   Abnormality of the gallbladder(HPO:0005264)
                      Abnormal gallbladder physiology(HPO:0012438)
                         Cholecystitis(HPO:0001082)
MedDRA:
Hepatobiliary disorders(MedDRA:10019805)
    Gallbladder disorders(MedDRA:10017628)
       Cholecystitis and cholelithiasis(MedDRA:10008616)
          Cholecystitis(HPO:0001082)
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Glycogen storage disease due to aldolase A deficiency (Orphanet:57)
Hemolytic anemia due to diphosphoglycerate mutase deficiency (Orphanet:714)
Hemolytic anemia due to glucophosphate isomerase deficiency (Orphanet:712)
Hemolytic anemia due to red cell pyruvate kinase deficiency (Orphanet:766)
Low phospholipid associated cholelithiasis (Orphanet:69663)
METACHROMATIC LEUKODYSTROPHY (OMIM:250100)
Non-spherocytic hemolytic anemia due to hexokinase deficiency (Orphanet:90031)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Triose phosphate-isomerase deficiency (Orphanet:868)